Prostate specific membrane antigen (psma) targeted nanoparticles for therapy of prostate cancer

ABSTRACT

The invention provides a nanoparticle composition that is decorated with a urea-based small-molecule peptidomimetic inhibitor of prostate specific membrane antigen (PSMA), which is expressed by almost all solid tumors. This strategy takes advantage of both the avidity of the functionalized nanoparticle for binding to PSMA and the ability of the nanoparticle to be retained for longer periods of time in the tumor due to enhanced leakage via EPR into the tumor interstitium and poor clearance due to underdeveloped or non-existent lymphatics within the tumor.

RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.12/744,982, filed Mar. 25, 2011, which is the 35 U.S.C. § 371 U.S.national entry of International Application PCT/US2008/013158 (WO2009/070302) having an International filing date of Nov. 26, 2008, whichclaims the benefit of U.S. Provisional Application Ser. No. 61/004,791,filed Nov. 30, 2007, the teachings of which are incorporated herein byreference in their entirety.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The present invention provides novel nanoparticle compositionscomprising a PSMA inhibitor, linker, nanoparticle and biologicallyactive compound. The compositions of the invention are useful forproviding methods of treating disorders, including cancer.

2. Background

Prostate cancer is the most commonly diagnosed non-cutaneous malignancyin American men and remains uniformly fatal once it undergoes metastasis(Jemal, A., et al. Cancer statistics, 2006. Ca-a Cancer Journal forClinicians, 56: 106-130, 2006). Androgen ablation therapy is effectivepalliative therapy, but in all men tumor progression eventually occurseven when completely androgen-deprived (e.g. inhibition of bothtesticular and adrenal androgens) (Crawford, E. D., et al. N Engl J Med,321: 419-424, 1989). Traditionally, prostate cancer was thought to berelatively resistant to cytotoxic chemotherapies administered followingandrogen ablation (Yagoda, A. and Petrylak, D. Cancer, 71: 1098-1109,1993). However, two recent studies demonstrated a modest survivalbenefit in men with hormone refractory metastatic disease treated withdocetaxel (Petrylak, D. P., et al. N Engl J Med, 351: 1513-1520, 2004;Tannock, I. F., et al. N Engl J Med, 351: 1502-1512, 2004). As withother cytotoxic therapies, docetaxel is associated with systemictoxicity that limits both the total dose and duration of therapy thatcan be administered (Petrylak, D. P., et al. N Engl J Med, 351:1513-1520, 2004; Tannock, I. F., et al. N Engl J Med, 351: 1502-1512,2004). To improve the therapeutic window, a number of approaches havebeen explored to target cytotoxic agents like docetaxel selectively totumor with the goal of higher tumor concentration and lessening oftoxicity to normal tissues. In this regard, various prostate tissuespecific surface proteins have been evaluated as potential bindingtargets to improve tumor uptake and retention of therapeutic agents.

The most extensively characterized surface protein has beenprostate-specific membrane antigen (PSMA). PSMA is highly expressed byprostate cancer compared to most normal tissue (Wright, G. L., et al.Urol Oncol, 1: 18-28, 1995; Israeli, R. S., et al. Cancer Res, 54:1807-1811, 1994; Chang, S. S., et al. Cancer Res, 59: 3192-3198, 1909;Silver, D. A., et al. Clin Cancer Res, 3: 81-85, 199. PSMA expressionhas also been demonstrated to increase following androgen ablation(Montgomery, B. T., et al. Prostate, 21: 63-73, 1992; Wright, G. L., etal. Urology, 48: 326-334, 1996). Multiple studies have documented thatPSMA is also expressed in the neovasculature of most solid tumors, butnot in the vasculature of normal tissues (Israeli, R. S., et al. CancerRes, 54: 1807-1811, 1994; Chang, S. S., et al. Cancer Res, 59:3192-3198, 1999). PSMA is a carboxypeptidase and is relatively unique inits ability to function as both an N-acetylated alpha-linked dipeptidaseand a gamma glutamyl (i.e. folate) hydrolase (Carter, R. E., et al. ProcNatl Acad Sci USA, 93: 749-753, 1996; Pinto, J. T., et al. Clin CancerRes, 2: 1445-1451, 1996). Therefore, PSMA has been an attractive targetfor both targeted drug delivery and imaging. PSMA targeting approachesinclude the use of PSMA peptide substrates (Mhaka, A., et al. CancerBiol Ther, 3: 551-558, 2004), PSMA-binding peptides (Aggarwal, S., etal. Cancer Res, 66: 9171-9177, 2006; Lupold, S. E. and Rodriguez, R. MolCancer Ther, 3: 597-603, 2004), RNA aptamers (Farokhzad, O. C., et al.Proc Natl Acad Sci USA, 103: 6315-6320, 2006; Lupold, S. E., et al.Cancer Res, 62: 4029-4033, 2002) or anti-PSMA monoclonalantibody-cytotoxin conjugates (Nanus, D. M., et al. J Urol, 170: S84-88;discussion S88-89, 2003). Efforts have also been made to imagePSMA-positive prostate tumors using labeled small-moleculepeptidomimetic PSMA inhibitors (Foss, C. A., et al. Clin Cancer Res, 11:4022-4028, 2005; Zhou, J., et al. Nat Rev Drug Discov, 4: 1015-1026,2005) and monoclonal antibodies (Bander, N. H. Nat Clin Pract Urol, 3:216-225, 2006; Lopes, A. D., et al. Cancer Res, 50: 6423-6429, 1990).

Previously Zhou et al reviewed a series of urea-based PSMA inhibitorswith high picomolar to low nanomolar K_(i) values (Zhou, J., et al. NatRev Drug Discov, 4: 1015-1026, 2005). Radiolabeled versions of theseinhibitors have been used to selectively image PSMA-expressing prostatecancer xenografts (Foss, C. A., et al. Clin Cancer Res, 11: 4022-4028,2005). On the basis of these studies, we developed an approach tofunctionalize nanoparticles with a highly potent urea-based PSMAinhibitor which could enable homing of the nanoparticle to prostatecancer. The small-molecule inhibitor would allow for the generation of ahighly decorated nanoparticle surface in which multiple ligand-proteinbinding interactions would produce an avidity effect that would enhancethe binding of the nanoparticle to PSMA.

In a previous study, it was demonstrated that docetaxel could be readilyencapsulated into poly(lactide-β-ethylene glycol-β-lactide)(PLA-PEG-PLA) nanoparticles and that these nanoparticles exhibited invivo efficacy (Chandran, S. S., Gerber, S. A., Rosen, M., and Denmeade,S. R. Formulation, in vitro efficacy and in vivo pharmacokinetics ofpolymeric nanoparticles bearing the natural toxin thapsigargin and itsanalog 12ADT. Manuscript in preparation). PLA-PEG-PLA was chosen as thecontrolled release system because its component polymers have beenpreviously demonstrated to be biocompatible and have been extensivelyused in drug development (Greenwald, R. B., et al. Adv Drug Deliv Rev,55: 217-250, 2003; Lee, J. S., et al. Eur J Pharm Biopharm, 59: 169-175,2005; Li, S. and McCarthy, S. Biomaterials, 20: 35-44, 1999; Shive, M.S. and Anderson, J. M. Adv Drug Deliv Rev, 28: 5-24, 1997).

What is desired is to provide novel nanoparticle compositions comprisinga biologically active material and PSMA inhibitors which are attached tothe nanoparticle via a linker, while retaining high affinity to PSMA.

SUMMARY OF THE INVENTION

In one aspect, the invention provides a nanoparticle compositioncomprising, a) a prostate specific membrane antigen (PSMA) inhibitor; b)a linker, c) a biologically active agent; and d) a nanoparticle.

In another aspect, the invention provides a method for treating orpreventing a disease or disorder in a subject, the method comprising thestep of administering to the subject a nanoparticle composition, suchthat the administration of the nanoparticle composition is effective totreat or prevent said disease or disorder, wherein the nanoparticlecomposition comprises a) a prostate specific membrane antigen (PSMA)inhibitor; b) a linker, c) a biologically active agent; and d) ananoparticle; or a nanoparticle composition of formula I:

(X)_(m)—(Y)_(n)—Z  (I);

wherein

X is an organic small molecule PSMA inhibitor;

Y is an organic linker;

Z is a nanoparticle comprising a biologically active agent;

m is 1-1000 and

n is 1-1000.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1: A general schematic demonstrating the binding of thenanoparticle. PSMA in dimeric form is observed on the cell surface. Thepolymeric nanoparticle has multiple PEG arms, some of which have thePSMA inhibitor attached to it. Total surface coverage by the inhibitorwas computed to be 2.23×10¹⁷ molecules/m² of surface area of thenanoparticles (˜30,000 inhibitor molecules/nanoparticle).

FIG. 2A depicts inhibition of activity of PSMA by FPPi and PEG. FPPiinhibits the activity of PSMA with an IC₅₀ in the range of 10 to 100ng/mL. In contrast, PEG inhibits the activity of PSMA by no more than10% at its highest concentration of FPPi tested suggesting specificinhibition (data not shown); FIG. 2B shows PSMA inhibition by polyPSMAi2when in free and nanoparticle form. There is a slight increase in theIC₅₀ when bound to the nanoparticle due to steric hindrance.

FIG. 3: Size distribution of nanoPSMAi2 as obtained by Light Scattering.The number average of size was estimated to be 222 nm. As observed, thenanoparticles are monodisperse with a polydispersity index of 0.131.

FIG. 4: In vitro toxicity of nontargeted and targeted nanoparticlesafter a 15 min incubation at a docetaxel concentration equivalent of 100nM. After 48 hour incubation, the treated arms show regression ingrowth. The effect is magnified with the higher incubation time of 96hours where the controls have expanded considerably, the nontargetednanoparticles demonstrate regression and the PSMA-targeted nanoparticlesnot only induce regression, but also reduce the overall cell number.Docetaxel was used as the control.

DETAILED DESCRIPTION OF THE INVENTION Definitions

As used herein a “nanoparticle” is a particle of submicron dimensions.Optionally, the nanoparticle is comprised of polymeric materials and maybe comprised of natural or synthetic polymeric materials. As usedherein, “synthetic polymeric materials” do not include natural polymers,such as proteins or starch. Examples of suitable polymeric materialsinclude, but are not limited to homopolymers, copolymers, randompolymers, graft polymers, alternating polymers, block polymers, branchpolymers, arborescent polymers and dendritic polymers. Nanoparticlesinclude nanospheres, which are nanoparticles having a substantiallyround, spherical or globular structure. Nanoparticles of the presentinvention may be used to carry therapeutic agents for delivery to targetcells or tissue. As used herein, carrying of a therapeutic agent by ananoparticle includes encapsulation of the therapeutic agent by thenanoparticle, or attachment, adsorbtion or other association of thetherapeutic agent to or with the nanoparticle. Suitably, nanoparticlesmay be biodegradable, for example being made of FDA-approved polymersand reagents for internal use. Nanoparticles may optionally comprisesurface ligands that enhance their transfer to target cells. Suitably,nanoparticles may be at least 20 nm, at least 25 nm, at least 35 nm, atleast 50 nm or at least 75 nm in average diameter. Suitably,nanoparticles may be less than 600 nm, less than 500 nm, less than 300nm, less than 250 nm, less than 200 nm, less than 150 nm or less than100 nm in average diameter. Suitably, nanoparticles are of a size thatdoes not induce an inflammatory response in the target cell.

As used herein, a “therapeutic agent” is an agent, or combination ofagents, that treats a cell, tissue or subject having a conditionrequiring therapy, when contacted with the cell, tissue or subject. Thetherapeutic agent may be suitably encapsulated, adsorbed or attached tothe nanoparticle. Non-limiting examples of suitable therapeutic agentsinclude small molecules, drugs, polypeptides, antagomirs, cytotoxicagents, chemotherapeutic agents, anti-angiogenic agents, radioactiveagents, imaging agents, cytokines, growth factors, apoptotic pathwayeffectors, agonists or antagonists, antibodies, radionuclides,anti-inflammatory agents, analgesics or polynucleotide sequences, orother agents disclosed herein.

As used herein, “alkyl” is intended to include both branched andstraight-chain saturated aliphatic hydrocarbon groups, having thespecified number of carbon atoms. Examples of alkyl include, but are notlimited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, s-butyl,t-butyl, n-pentyl, and s-pentyl. Preferred alkyl groups are C₁₋₁₂ alkylgroups. Especially preferred alkyl groups are methyl, ethyl, propyl,butyl, and 3-pentyl.

“Alkenyl” is intended to include hydrocarbon chains of either a straightor branched configuration comprising one or more unsaturatedcarbon-carbon bonds, which may occur in any stable point along thechain, such as ethenyl and propenyl. Alkenyl groups typically will have2 to about 12 carbon atoms.

“Alkynyl” is intended to include hydrocarbon chains of either a straightor branched configuration comprising one or more carbon-carbon triplebonds, which may occur in any stable point along the chain, such asethynyl and propynyl. Alkynyl groups typically will have 2 to about 12carbon atoms.

As used herein, the term “aryl” includes groups that contain 1 to 3separate or fused rings and from 6 to about 18 ring atoms, withouthetero atoms as ring members. Specifically preferred carbocyclic arylgroups include phenyl, and naphthyl including 1-napthyl and 2-naphthyl.

The term “aralkyl” or “arylalkyl” refers to an alkyl residue attached toan aryl ring. Examples of aralkyl include, but are not limited to,benzyl, phenethyl and the like. The term “heteroaralkyl” or“heteroarylalkyl” refers to an alkyl residue attached to a heteroarylring. Examples include, but are not limited to, pyridinylmethyl,pyrimidinylethyl and the like.

“Haloalkyl” is intended to include both branched and straight-chainsaturated aliphatic hydrocarbon groups having the specified number ofcarbon atoms, substituted with 1 or more halogen atoms. Examples ofhaloalkyl include, but are not limited to, mono-, di-, ortri-fluoromethyl, mono-, di-, or tri-chloromethyl, mono-, di-, tri-,tetra-, or penta-fluoroethyl, and mono-, di-, tri-, tetra-, orpenta-chloroethyl. Typical haloalkyl groups will have 1 to about 2carbon atoms.

“Alkoxy” represents an alkyl group as defined above with the indicatednumber of carbon atoms attached through an oxygen bridge. Examples ofalkoxy include, but are not limited to, methoxy, ethoxy, n-propoxy,i-propoxy, n-butoxy, 2-butoxy, t-butoxy, n-pentoxy, 2-pentoxy,3-pentoxy, isopentoxy, neopentoxy, n-hexoxy, 2-hexoxy, 3-hexoxy, and3-methylpentoxy. Alkoxy groups typically have 1 to about 12 carbonatoms.

“Haloalkoxy” represents a haloalkyl group as defined above with theindicated number of carbon atoms attached through an oxygen bridge.

As used herein, the term “alkylthio” includes those groups having one ormore thioether linkages and preferably from 1 to about 12 carbon atoms.

As used herein, the term “alkylsulfinyl” includes those groups havingone or more sulfoxide (SO) linkage groups and typically from 1 to about12 carbon atoms.

As used herein, the term “alkylsulfonyl” includes those groups havingone or more sulfonyl (SO₂) linkage groups and typically from 1 to about12 carbon atoms.

As used herein, the term “alkylamino” includes those groups having oneor more primary, secondary and/or tertiary amine groups and typicallyfrom 1 to about 12 carbon atoms.

“Halo,” “hal,” or “halogen” as used herein refers to fluoro, chloro,bromo, or iodo; and “counter-ion” is used to represent a small,negatively charged species such as chloride, bromide, hydroxide,acetate, sulfate, and the like.

As used herein, “cycloalkyl” or “carbocyclic” group are usedinterchangeably and are intended to mean any stable 3- to 7-memberedmonocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic group,any of which may be saturated or partially unsaturated. In addition tothose exemplified elsewhere herein, examples of such carbocyclesinclude, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctanyl,[4.3.0]bicyclononanyl, [4.4.0]bicyclodecanyl, [2.2.2]bicyclooctanyl,fluorenyl, indanyl, and tetrahydronaphthyl.

As used herein, the term “heterocyclic” or “heterocycloalkyl” isintended to include saturated, or partially unsaturated groups having 1to 3 (preferably fused) rings with 3 to about 8 members per ring atleast one ring containing an atom selected from N, O or S. The nitrogenand sulfur heteroatoms may optionally be oxidized.

As used herein, the term “heteroaryl” is intended to include cyclicunsaturated (aromatic) groups having 1 to 3 (preferably fused) ringswith 3 to about 8 members per ring at least one ring containing an atomselected from N, O or S. The nitrogen and sulfur heteroatoms mayoptionally be oxidized.

Examples of heterocyclic and heteroaryl groups include, but are notlimited to, those exemplified elsewhere herein and further includeacridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl,benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl,benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl,carbazolyl, NH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl,decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl,dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl,imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl,indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl,isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl,isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl,oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl;-1,2,5oxadiazolyl,1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinyl, pyrimidinyl,phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl,phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl,pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl,pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole,pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl,pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl,quinuclidinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl,tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl,1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4thiadiazolyl, thianthrenyl,thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl,thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl,1,2,5-triazolyl, 1,3,4-triazolyl, and xanthenyl.

Preferred heterocyclic and heteroaryl groups include, but are notlimited to, pyridinyl, pyrimidinyl, furanyl, thienyl, pyrrolyl,pyrazolyl, pyrrolidinyl, morpholinyl, piperidinyl, piperazinyl, andimidazolyl. Also included are fused ring and spiro compounds containing,for example, the above heterocycles.

In certain instances, any of the groups described above may be bonded totwo separate groups, e.g., an alkyl group includes alkenylene groups,e.g., —CH₂—, —CH₂CH₂—, and the like.

The term “leaving group,” or “LG”, as used herein, refers to any groupthat leaves in the course of a chemical reaction involving the group andincludes but is not limited to halogen, brosylate, mesylate, tosylate,triflate, p-nitrobenzoate, phosphonate groups, for example.

The terms “optionally substituted”, “optionally substituted alkyl,”“optionally substituted “optionally substituted alkenyl,” “optionallysubstituted alkynyl”, “optionally substituted cycloalkyl,” “optionallysubstituted cycloalkenyl,” “optionally substituted aryl”, “optionallysubstituted heteroaryl,” “optionally substituted aralkyl”, “optionallysubstituted heteroaralkyl,” “optionally substituted heterocycloalkyl,”and any other optionally substituted group as used herein, refer togroups that are substituted or unsubstituted by independent replacementof one, two, or three or more of the hydrogen atoms thereon withsubstituents including, but not limited to: —F, —Cl, —Br, —I, —OH,protected hydroxy, —NO₂, —CN, —NH₂, protected amino, —NH—C₁-C₁₂-alkyl,—NH—C₂-C₁₂-alkenyl, —NH—C₂-C₁₂-alkenyl, —NH—C₃-C₁₂-cycloalkyl, —NH-aryl,—NH-heteroaryl, —NH-heterocycloalkyl, -dialkylamino, -diarylamino,-dihetero arylamino, —O—C₁-C₁₂-alkyl, —O—C₂-C₁₂-alkenyl,—O—C₂-C₁₂-alkenyl, —O—C₃-C₁₂-cycloalkyl, —O-aryl, —O-heteroaryl,—O-heterocycloalkyl, —C(O)—C₁-C₁₂-alkyl, —C(O)—C₂-C₁₂-alkenyl, —C(O)—C₂-C₁₂-alkenyl, —C(O)—C₃-C₁₂-cycloalkyl, —C(O)-aryl, —C(O)— heteroaryl,—C(O)-heterocycloalkyl, —CONH₂, —CONH—C₁-C₁₂-alkyl,—CONH—C₂-C₁₂-alkenyl, —CONH—C₂-C₁₂-alkenyl, —CONH—C₃-C₁₂-cycloalkyl,—CONH-aryl, —CONH— heteroaryl, —CONH-heterocycloalkyl,—OCO₂—C₁-C₁₂-alkyl, —OCO₂—C₂-C₁₂-alkenyl, —OCO₂—C₂-C₁₂-alkenyl,—OCO₂—C₃-C₁₂-cycloalkyl, —OCO₂-aryl, —OCO₂-heteroaryl,—OCO₂-heterocycloalkyl, —OCONH₂, —OCONH—C₁-C₁₂-alkyl,—OCONH—C₂-C₁₂-alkenyl, —OCONH—C₂-C₁₂-alkenyl, —OCONH—C₃-C₁₂-cycloalkyl,—OCONH— aryl, —OCONH— heteroaryl, —OCONH— heterocycloalkyl,—NHC(O)—C₁-C₁₂-alkyl, —NHC(O)—C₂-C₁₂-alkenyl, —NHC(O)—C₂-C₁₂-alkenyl,—NHC(O)—C₃-C₁₂-cycloalkyl, —NHC(O)-aryl, —NHC(O)-heteroaryl,—NHC(O)-heterocycloalkyl, —NHCO₂—C₁-C₁₂-alkyl, —NHCO₂—C₂-C₁₂-alkenyl,—NHCO₂—C₂-C₁₂-alkenyl, —NHCO₂—C₃-C₁₂-cycloalkyl, —NHCO₂— aryl, —NHCO₂—heteroaryl, —NHCO₂— heterocycloalkyl, —NHC(O)NH₂,—NHC(O)NH—C₁-C₁₂-alkyl, —NHC(O)NH—C₂-C₁₂-alkenyl,—NHC(O)NH—C₂-C₁₂-alkenyl, —NHC(O)NH—C₃-C₁₂-cycloalkyl, —NHC(O)NH-aryl,—NHC(O)NH-heteroaryl, —NHC(O)NH-heterocycloalkyl, NHC(S)NH₂,—NHC(S)NH—C₁-C₁₂-alkyl, —NHC(S)NH—C₂-C₁₂-alkenyl,—NHC(S)NH—C₂-C₁₂-alkenyl, —NHC(S)NH—C₃-C₁₂-cycloalkyl, —NHC(S)NH-aryl,—NHC(S)NH-heteroaryl, —NHC(S)NH-heterocycloalkyl, —NHC(NH)NH₂,—NHC(NH)NH—C₁-C₁₂-alkyl, —NHC(NH)NH—C₂-C₁₂-alkenyl,—NHC(NH)NH—C₂-C₁₂-alkenyl, —NHC(NH)NH—C₃-C₁₂-cycloalkyl,—NHC(NH)NH-aryl, —NHC(NH)NH-heteroaryl, —NHC(NH)NH-heterocycloalkyl,—NHC(NH)—C₁-C₁₂-alkyl, —NHC(NH)—C₂-C₁₂-alkenyl, —NHC(NH)—C₂-C₁₂-alkenyl,—NHC(NH)—C₃-C₁₂-cycloalkyl, —NHC(NH)-aryl, —NHC(NH)-heteroaryl,—NHC(NH)-heterocycloalkyl, —C(NH)NH—C₁-C₁₂-alkyl,—C(NH)NH—C₂-C₁₂-alkenyl, —C(NH)NH—C₂-C₁₂-alkenyl,—C(NH)NH—C₃-C₁₂-cycloalkyl, —C(NH)NH-aryl, —C(NH)NH-heteroaryl,—C(NH)NH— heterocycloalkyl, —S(O)—C₁-C₁₂-alkyl, —S(O)—C₂-C₁₂-alkenyl,—S(O)—C₂-C₁₂-alkenyl, —S(O)—C₃-C₁₂-cycloalkyl, —S(O)-aryl,—S(O)-heteroaryl, —S(O)-heterocycloalkyl—SO₂NH₂, —SO₂NH—C₁-C₁₂-alkyl,—SO₂NH—C₂-C₁₂-alkenyl, —SO₂NH—C₂-C₁₂-alkenyl, —SO₂NH—C₃-C₁₂-cycloalkyl,—SO₂NH— aryl, —SO₂NH— heteroaryl, —SO₂NH— heterocycloalkyl,—NHSO₂—C₁-C₁₂-alkyl, —NHSO₂—C₂-C₁₂-alkenyl, —NHSO₂—C₂-C₁₂-alkenyl,—NHSO₂—C₃-C₁₂-cycloalkyl, —NHSO₂-aryl, —NHSO₂-heteroaryl, —NHSO₂—heterocycloalkyl, —CH₂NH₂, —CH₂SO₂CH₃, -aryl, -arylalkyl, -heteroaryl,-heteroarylalkyl, -heterocycloalkyl, —C₃-C₁₂-cycloalkyl,polyalkoxyalkyl, polyalkoxy, -methoxymethoxy, -methoxyethoxy, —SH,—S—C₁-C₁₂-alkyl, —S—C₂-C₁₂-alkenyl, —S—C₂-C₁₂-alkenyl,—S—C₃-C₁₂-cycloalkyl, —S-aryl, —S-heteroaryl, —S-heterocycloalkyl, ormethylthiomethyl.

It is understood that the aryls, heteroaryls, alkyls, and the like canbe further substituted. In accordance with the invention, any of thearyls, substituted aryls, heteroaryls and substituted heteroarylsdescribed herein, can be any aromatic group. Aromatic groups can besubstituted or unsubstituted.

A “pharmaceutically acceptable carrier” refers to a biocompatiblesolution, having due regard to sterility, pH, isotonicity, stability,and the like and can include any and all solvents, diluents (includingsterile saline, Sodium Chloride Injection, Ringer's Injection, DextroseInjection, Dextrose and Sodium Chloride Injection, Lactated Ringer'sInjection and other aqueous buffer solutions), dispersion media,coatings, antibacterial and antifungal agents, isotonic agents, and thelike. The pharmaceutically acceptable carrier may also containstabilizers, preservatives, antioxidants, or other additives, which arewell known to one of skill in the art, or other vehicle as known in theart.

As used herein, “pharmaceutically acceptable salts” refer to derivativesof the disclosed compounds wherein the parent compound is modified bymaking non-toxic acid or base salts thereof. Examples ofpharmaceutically acceptable salts include, but are not limited to,mineral or organic acid salts of basic residues such as amines; alkalior organic salts of acidic residues such as carboxylic acids; and thelike. The pharmaceutically acceptable salts include the conventionalnon-toxic salts or the quaternary ammonium salts of the parent compoundformed, for example, from non-toxic inorganic or organic acids. Forexample, conventional non-toxic acid salts include those derived frominorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic,phosphoric, nitric and the like; and the salts prepared from organicacids such as acetic, propionic, succinic, glycolic, stearic, lactic,malic, tartaric, citric, ascorbic, pamoic, malefic, hydroxymaleic,phenylacetic, glutamic, benzoic, salicylic, mesylic, sulfanilic,2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethanedisulfonic, oxalic, isethionic, HOOC—(CH₂)n-COOH where n is 0-4, and thelike. The pharmaceutically acceptable salts of the present invention canbe synthesized from a parent compound that contains a basic or acidicmoiety by conventional chemical methods. Generally, such salts can beprepared by reacting free acid forms of these compounds with astoichiometric amount of the appropriate base (such as Na, Ca, Mg, or Khydroxide, carbonate, bicarbonate, or the like), or by reacting freebase forms of these compounds with a stoichiometric amount of theappropriate acid. Such reactions are typically carried out in water orin an organic solvent, or in a mixture of the two. Generally,non-aqueous media like ether, ethyl acetate, ethanol, isopropanol, oracetonitrile are preferred, where practicable. Lists of additionalsuitable salts may be found, e.g., in Remington's PharmaceuticalSciences, 17th ed., Mack Publishing Company, Easton, Pa., p. 1418(1985).

The term “subject” as used herein refers to a mammal. A subjecttherefore refers to, for example, dogs, cats, horses, cows, pigs, guineapigs, and the like. Preferably the subject is a human. When the subjectis a human, the subject may be either a patient or a healthy human.

Compositions of the Invention

In one aspect, the invention provides a nanoparticle compositioncomprising, a) a prostate specific membrane antigen (PSMA) inhibitor; b)a linker, c) a biologically active agent; and d) a nanoparticle.

In one embodiment, the invention provides a nanoparticle compositionwherein the PSMA inhibitor is attached to a linker.

In another embodiment, the invention provides a nanoparticle compositionwherein the biologically active agent is encapsulated in thenanoparticle.

In certain embodiments, the invention provides a nanoparticlecomposition wherein the linker is attached to the nanoparticle.

In one embodiment, the invention provides a nanoparticle composition offormula I:

(X)_(m)—(Y)_(n)—Z  (I);

wherein

X is an organic small molecule PSMA inhibitor;

Y is an organic linker;

Z is a nanoparticle comprising a biologically active agent;

m is 1-1000 and

n is 1-1000.

In certain embodiments, X is a compound of formula II,

wherein,

R₁ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic;

R₂ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,optionally substituted alkylcarboxy, or optionally substitutedcarbocyclic;

R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic;

or a pharmaceutically acceptable salt thereof.

In other embodiments, R′ and R″ are each independently —OR₄.

In another embodiment, each R₄ is independently H, methyl, or ethyl.

In certain embodiments, R₁ is a side chain of a naturally occurringamino acid.

In other embodiments, R₁ is optionally substituted alkyl, containing 0,1, 2, or 3 heteroatoms selected from O, S, or N; optionally substitutedarylalkyl, optionally substituted alkoxy, or optionally substitutedheterocyclic.

In a further embodiment, R₁ is (CH₂)_(p)—O—Y, (CH₂)_(p)—S—Y,(CH₂)_(p)—SO—Y, (CH₂)_(p)—SO₂—Y, (CH₂)_(p)—N(R₃)S(O)₂—Y,(CH₂)_(p)—N(R₃)(SO₂)NR₃—Y, (CH₂)_(p)—NR₃—Y, (CH₂)_(p)—C(O)—O—Y,(CH₂)_(p)—C(O)—Y, (CH₂)_(p)—C(O)NR₃—Y, or (CH₂)_(p)—N(R₃)C(O)—Y;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic; and

p is 1-6.

In still a further embodiment, R₁ is (CH₂)_(p)—O—Y, (CH₂)_(p)—NR₃—Y,(CH₂)_(p)—C(O)—O—Y, (CH₂)_(p)—C(O)—Y, (CH₂)_(p)—C(O)NR₃—Y, or(CH₂)_(p)—N(R₃)C(O)—Y;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic; and

p is 3-6.

In a further embodiment, R₁ is (CH₂)_(p)—NR₃—Y.

In another embodiment, R₂ is optionally substituted alkyl, containing 0,1, 2, or 3 heteroatoms selected from O, S, or N; or optionallysubstituted arylalkyl.

In certain embodiments, R₂ is a side chain of a naturally occurringamino acid.

In a further embodiment, R₂ is (CH₂)_(p)—OR₄, (CH₂)_(p)—SR₄,(CH₂)_(p)—SOR₄, (CH₂)_(p)—SO₂R₄, (CH₂)_(p)—N(R₃)S(O)₂—R₄,(CH₂)_(p)—N(R₃)(SO₂)NR₃R₄, (CH₂)_(p)—NR₃R₄, (CH₂)_(p)—C(O)—O—R₄,(CH₂)_(p)—C(O)R₄, (CH₂)_(p)—C(O)NR₃R₄, or (CH₂)_(p)—N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic; and

p is 1-6.

In a further embodiment, R₂ is (CH₂)_(p)—OR₄, (CH₂)_(p)—C(O)—O—R₄,(CH₂)_(p)—C(O)R₄, (CH₂)_(p)—C(O)NR₃R₄, or (CH₂)_(p)—N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic; and

p is 1-3.

In a further embodiment, R₂ is (CH₂)_(p)—C(O)—O—R₄.

In certain embodiments, Y is

wherein

A is O, S, NH, N(alkyl) or N(aryl); and

R_(A) is optionally substituted alkyl, optionally substituted alkenyl oroptionally substituted alkynyl, each containing heteroatoms selectedfrom O, S, or N.

In one embodiment, A is C═O.

In another embodiment, R_(A) is (CH₂)_(r)-Q-Z, (CH₂O)_(r)-Q-Z,(CH₂NH)_(r)-Q-Z, (CH₂NR_(B))_(r)-Q-Z, or combinations thereof,

wherein

Q is CO, C(O)O, C(O)NH, C(O)NR_(B), OCO, OC(O)O, OC(O)NH, OC(O)NR_(B),NHCO, NHC(O)O, NHC(O)NH, NHC(O)NR_(B), NR_(B)CO, NR_(B)C(O)O,NR_(B)C(O)NH, NR_(B)C(O)NR_(B), CS, C(S)O, C(S)NH, C(S)NR_(B), OCS,OC(S)O, OC(S)NH, OC(S)NR_(B), NHCS, NHC(S)O, NHC(S)NH, NHC(S)NR_(B),NR_(B)CS, NR_(B)C(S)O, NR_(B)C(S)NH, NR_(B)C(S)NR_(B);

each R_(B) is independently optionally substituted alkyl or optionallysubstituted aryl; and

r is 3-20.

In a further embodiment, Q is C(O)O, NHC(S)NH, or NHC(O)NH.

In one embodiment, Z is a nanoparticle comprisingPoly-lactide-b-ethylene glycol-b-lactide (PLA-PEG-PLA), polylactide(PLA), polyglycolide, polylactide-polyglycolide,poly(lactide-co-glycolide), polyethylene glycol-co-lactide (PEG-PLA),poly(lactic-co-glycolic acid), polyhydroxybutyric acid,polyhydroxyvaleric acid, polycaprolactone, polyesteramide,polycyanoacrylate, poly(amino acids), polycarbonate, polyanhydride, polyalkylcyanoacrylate, polyethylene glycol (PEG), polysialic acid,polylactic (polylactide), polyglycolic acid (polyglycolide),apolylactic-polyglycolic acid, polyvinyl alcohol, polyvinylpyrrolidone,polymethoxazoline, polyethyloxazoline, polyhydroxyethyloxazoline,polyhydroxypropyloxazoline, polyaspartamide, polyhydroxypropylmethacrylamide, polymethacrylamide, polydimethylacrylamide,polyvinylmethylether, polyhydroxyethyl acrylate, derivatized cellulosessuch as hydroxymethylcellulose or hydroxyethylcellulose,methoxypolyethylene glycol, avidin, biotin, or combinations thereof.

In a further embodiment, Z is a nanoparticle comprisingPoly-lactide-b-ethylene glycol-b-lactide (PLA-PEG-PLA), polylactide(PLA), polyglycolide, polylactide-polyglycolide,poly(lactide-co-glycolide), polyethylene glycol-co-lactide (PEG-PLA), orcombinations thereof.

In another embodiment, Z comprises one or more polymers, wherein the oneor more polymers have an average molecular weight from about 2,000 Da toabout 5,000 Da.

In other embodiments, the nanoparticle has a diameter ranging from about1 nm to about 500 nm. In certain embodiments, the diameter of thenanoparticle ranges from about 10 nm to about 250 nm; about 25 nm toabout 200 nm; or about 10 nm to about 50 nm.

In another embodiment, the biologically active agent is selected from anucleic acid, a polynucleotide, an amino acid, a peptide a protein, apolypeptide, a carbohydrate, a lipid, a glycoprotein, a glycan, alipoprotein, and a small molecule.

In certain embodiments, the biologically active agent is a knownpharmaceutical.

In a further embodiment, the biologically active agent is selected froman anti-AIDS agent, anti-cancer agent, antibiotic, antioxidants,immunosuppressant, anti-viral agent, enzyme inhibitor, proteaseinhibitor, reverse transcriptase inhibitor, fusion inhibitor,neurotoxin, opiod, hypnotic, anti-histamine, lubricant, tranquilizer,anti-convulsant, muscle relaxant, anti-Parkinson agent, anti-spasmodic,muscle contractant, channel blocker, miotic, anti-cholinergic,anti-glaucoma agent, anti-parasite, anti-protozoal, modulator ofcell-extracellular matrix interaction, cell growth inhibitor,anti-adhesion agent, vasodilating agent, inhibitor of DNA, inhibitor ofRNA, inhibitor of protein synthesis, inhibitors of apoptotic genes,modulators of transcription factors, anti-hypertensive, analgesic,anti-pyretic, steroidal anti-inflammatory agent, non steroidalanti-inflammatory agent, anti-angiogenic, anti-secretory, anticoagulant,antithrombotic agent, local anesthetic, ophthalmic, prostaglandin,anti-depressant, anti-psychotic, anti-emetic, antiproliferative,antimigration, antiangiogenic, antithrombotic, anti-inflammatory,antiphlogistic, cytostatic, cytotoxic, anticoagulative, antibacterial,antiviral and/or antimycotic agent and an imaging agent.

In a further embodiment, the biologically active agent is selected fromactinomycin D, ametantrone, 9-Aminocamptothecin, aminoglutethimide,amsacrine, anastrozole, antagonists of purine and pyrimidine bases,anthracycline, aromatase inhibitors, asparaginase, antiestrogens,bendamustine, bexarotene, biolimus A9, bleomycin, buserelin, busulfan,calicheamicins, camptothecin, camptothecin derivatives, capecitabine,carboplatin, carmustine, chlorambucil, cisplatin, cladribine,cyclophosphamide, cytarabine, cytosine arabinoside, alkylatingcytostatics, dacarbazine, dactinomycin, daunorubicin,5′-deoxy-5-fluorouridine, docetaxel, doxorubicin (adriamycin),doxorubicin lipo, epirubicin, estramustine, etoposide, exemestane,fludarabine, fluorouracil, folic acid antagonists, formestane,gemcitabine, glucocorticoids, goserelin, hormones and hormoneantagonists, hycamtin, hydroxyurea, idarubicin, ifosfamide, imatinib,irinotecan, letrozole, leuprorelin, lomustine, maytansinoids, melphalan,mercaptopurine, methotrexate, miltefosine, mitomycins, mitopodozide,antimitotic agents, mitoxantrone, nimustine, oxaliplatin,oxazaphosphorines, paclitaxel, pentostatin, podophyllotoxin derivatives,procarbazine, rapamycin, rhodomycin D, tamoxifen, temozolomide,teniposide, testolactone, thiotepa, thioguanine, topoisomeraseinhibitors, topotecan, treosulfan, tretinoin, triptorelin,trofosfamides, vinca alkaloids, vinblastine, vincristine, vindesine,vinorelbine, cytostatically active antibiotics, chlorethamine,cyclophosphamide, trofosfamide, ifosfamide, melphalan, chlorambucil,busulfan, thiotepa, carmustine, lomustine, dacarbazine, procarbazine,temozolomide, treosulfan, estramustine, nimustine, daunorubicin,doxorubicin (adriamycin), dactinomycin, mitomycin C, bleomycin,epirubicin (4-epi-adriamycin), idarubicin, mitoxantrone, amsacrine,actinomycin D, methotrexate, 5-fluorouracil, 6-thioguanin,6-mercaptopurine, fludarabine, cladribine, pentostatin, gemcitabine,cytarabine, azathioprine, raltitrexed, capecitabine, cytosinearabinoside, thioguanine, mercaptopurine, vincristine, vinblastine,vindesine, etoposide, alkaloids, podophyllotoxins, cisplatin,carboplatin, oxaliplatin, vincristine, vinblastine, vindesine,vinorelbine, Taxol®, etoposide, teniposide, camptothecin, topotecan,irinotecan, hydroxycarbamide (hydroxyurea), imatinib, Miltefosine®,amsacrine, topotecan (inhibitor of topoisomerase-I), pentostatin,bexarotene, biolimus A9, rapamycin (sirolimus), rhodomycin D,ametantrone, bendamustine, oxazaphosphorine, 5′-deoxy-5-fluorouridine,9-aminocamptothecin, podophyllotoxin derivatives, mitopodozide, vincaalkaloids, calicheamicins, maytansinoids, tretinoin, asparaginase,trastuzumab (Herceptin®), alemtuzumab (MabCampath®) and rituximab(MabThera®), glucocorticoids, prednisone, estrogens, fosfestrol,estramustine, LHRH, buserelin, goserelin, leuprorelin, triptorelin,flutamide, cyproterone acetate, tamoxifen, toremifen, aminoglutethimide,formestane, exemestane, letrozole, anastrozole, Cu/Zn SOD, glutathione,anti-apoptotic polypeptides.

In certain embodiments, the biologically active agent is docetaxel.

In another embodiment, the invention provides a nanoparticle compositionof formula III:

wherein,

R₁ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic;

R₂ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,optionally substituted alkylcarboxy, or optionally substitutedcarbocyclic;

R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic;

A is O, S, NH, N(alkyl) or N(aryl); and

R_(A) is optionally substituted alkyl, optionally substituted alkenyl oroptionally substituted alkynyl, each containing heteroatoms selectedfrom O, S, or N;

Z is a nanoparticle comprising a biologically active agent; and

q is 1-1000;

or a pharmaceutically acceptable salt thereof.

In one embodiment, R′ and R″ are each independently —OR₄; and each R₄ isindependently H, methyl, or ethyl.

In another embodiment, R₁ is optionally substituted alkyl, containing 0,1, 2, or 3 heteroatoms selected from O, S, or N; optionally substitutedarylalkyl, optionally substituted alkoxy, or optionally substitutedheterocyclic.

In a further embodiment, R₁ is (CH₂)_(p)—O—, (CH₂)_(p)—NR₃—,(CH₂)_(p)—C(O)—O—, (CH₂)_(p)—C(O)—, (CH₂)_(p)—C(O)NR₃—, or(CH₂)_(p)—N(R₃)C(O)—; R₃ and R₄ are each independently selected at eachoccurrence from the following: H, optionally substituted alkyl,optionally substituted alkenyl or optionally substituted alkynyl, eachcontaining 0, 1, 2, or 3 heteroatoms selected from O, S, or N;optionally substituted aryl; optionally substituted heteroaryl;optionally substituted heterocyclic; or optionally substitutedcarbocyclic; and

p is 3-6.

In certain embodiments, R₁ is (CH₂)_(p)—NR₃—.

In one embodiment, R₂ is optionally substituted alkyl, containing 0, 1,2, or 3 heteroatoms selected from O, S, or N; or optionally substitutedarylalkyl.

In a further embodiment, R₂ is (CH₂)_(p)—OR₄, (CH₂)_(p)—C(O)—O—R₄,(CH₂)_(p)—C(O)R₄, (CH₂)_(p)—C(O)NR₃R₄, or (CH₂)_(p)—N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic; and

p is 1-3.

In a further embodiment, R₂ is (CH₂)_(p)—C(O)—O—R₄.

In certain embodiments, A is C═O; R_(A) is (CH₂)_(r)-Q-, (CH₂O)_(r)-Q-,(CH₂NH)_(r)-Q-, (CH₂NR_(B))_(r)-Q-, or combinations thereof,

wherein

Q is CO, C(O)O, C(O)NH, C(O)NR_(B), OCO, OC(O)O, OC(O)NH, OC(O)NR_(B),NHCO, NHC(O)O, NHC(O)NH, NHC(O)NR_(B), NR_(B)CO, NR_(B)C(O)O,NR_(B)C(O)NH, NR_(B)C(O)NR_(B), CS, C(S)O, C(S)NH, C(S)NR_(B), OCS,OC(S)O, OC(S)NH, OC(S)NR_(B), NHCS, NHC(S)O, NHC(S)NH, NHC(S)NR_(B),NR_(B)CS, NR_(B)C(S)O, NR_(B)C(S)NH, NR_(B)C(S)NR_(B);

each R_(B) is independently optionally substituted alkyl or optionallysubstituted aryl; and

r is 3-20.

In a further embodiment, Q is C(O)O, NHC(S)NH, or NHC(O)NH.

In certain embodiments, Z is a nanoparticle comprisingPoly-lactide-b-ethylene glycol-b-lactide (PLA-PEG-PLA), polylactide(PLA), polyglycolide, polylactide-polyglycolide,poly(lactide-co-glycolide), polyethylene glycol-co-lactide (PEG-PLA), orcombinations thereof.

In another embodiment, the invention provides a nanoparticle compositionof formula IV:

wherein,

R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic;

R_(A) is optionally substituted alkyl, optionally substituted alkenyl oroptionally substituted alkynyl, each containing heteroatoms selectedfrom O, S, or N;

Z is a nanoparticle comprising a biologically active agent; and

q is 1-1000;

or a pharmaceutically acceptable salt thereof.

In one embodiment, R′ and R″ are each independently —OR₄; and each R₄ isindependently H, methyl, or ethyl.

In another embodiment, R_(A) is (CH₂)_(r)-Q-, (CH₂O)_(r)-Q-,(CH₂NH)_(r)-Q-, (CH₂NR_(B))_(r)-Q-, or combinations thereof,

wherein

Q is CO, C(O)O, C(O)NH, C(O)NR_(B), OCO, OC(O)O, OC(O)NH, OC(O)NR_(B),NHCO, NHC(O)O, NHC(O)NH, NHC(O)NR_(B), NR_(B)CO, NR_(B)C(O)O,NR_(B)C(O)NH, NR_(B)C(O)NR_(B), CS, C(S)O, C(S)NH, C(S)NR_(B), OCS,OC(S)O, OC(S)NH, OC(S)NR_(B), NHCS, NHC(S)O, NHC(S)NH, NHC(S)NR_(B),NR_(B)CS, NR_(B)C(S)O, NR_(B)C(S)NH, NR_(B)C(S)NR_(B);

each R_(B) is independently optionally substituted alkyl or optionallysubstituted aryl; and

r is 3-20.

In a further embodiment, Q is C(O)O, NHC(S)NH, or NHC(O)NH.

In one embodiment, Z is a nanoparticle comprisingPoly-lactide-b-ethylene glycol-b-lactide (PLA-PEG-PLA), polylactide(PLA), polyglycolide, polylactide-polyglycolide,poly(lactide-co-glycolide), polyethylene glycol-co-lactide (PEG-PLA), orcombinations thereof.

The compounds and compositions herein described may have one or moreasymmetric centers or planes. Compounds of the present inventioncontaining an asymmetrically substituted atom may be isolated inoptically active or racemic forms. It is well known in the art how toprepare optically active forms, such as by resolution of racemic forms(racemates), by asymmetric synthesis, or by synthesis from opticallyactive starting materials. Resolution of the racemates can beaccomplished, for example, by conventional methods such ascrystallization in the presence of a resolving agent, or chromatography,using, for example a chiral HPLC column. Many geometric isomers ofolefins, C═N double bonds, and the like can also be present in thecompounds described herein, and all such stable isomers are contemplatedin the present invention. Cis and trans geometric isomers of thecompounds of the present invention are described and may be isolated asa mixture of isomers or as separated isomeric forms. All chiral(enantiomeric and diastereomeric), and racemic forms, as well as allgeometric isomeric forms of a structure are intended, unless thespecific stereochemistry or isomeric form is specifically indicated.

Nanoparticles may be synthesized using any method described in the art,or disclosed herein. In one embodiment, nanoparticles are modified bypolyethylene glycol (PEG) conjugation, a process known in the art as“PEGylation.” In certain embodiments, nanoparticles may be suitably madeusing polygycolic acid (PGA) and/or poly-lactic acid (PLA) to form apolymer or copolymer used to construct the nanoparticle matrix.Nanoparticle uptake and transfection into specific cells is enhanced bycomplexing nanoparticles to ligands specific to PSMA. Additional methodsof increasing exposure to PSMA includes changes to PEG surface densitywhich may be optionally modified to uncover the hydrophobic and chargedpolymeric core, or PEG carrier hydrolysis to expose the hydrophobic coreof the nanoparticle.

In one embodiment, a PEG arm was introduced as a spacer using anα-amino-ω-hydroxy terminated poly(ethylene glycol-b-ε-caprolactone)(PEG-PCL) polymer chain in order to maintain sufficient distance betweenthe small-molecule PSMA inhibitor and the nanoparticle surface. PEGfunctions in this targeting application to decrease nonspecific proteinbinding (i.e. ‘bio-fouling’) and minimizes particle clearance by thereticuloendothelial system. Additionally, the PEG-PCL would partitionsuch that the PEG would orient towards the surface of the nanoparticlethus improving presentation of the attached binding ligand. Using thisrationale, a strategy was developed to generate a PEGylated urea-basedPSMA inhibitor incorporated into a PLA-PEG-PLA nanoparticle, as shown inFIG. 1. The components of this system and the PSMA inhibitor conjugatednanoparticles were then characterized for their ability to inhibit theenzymatic activity of PSMA. Subsequently, docetaxel encapsulated,PSMA-targeted nanoparticles were evaluated for their ability to bind toPSMA expressing human LNCaP prostate cancer cells and to selectivelyinhibit their growth in vitro.

Targeted therapy for cancer has gained considerable importance recentlywith various improvements not only in target identification, but also insmall-molecule or antibody development. It has also been demonstratedthat polymeric nanoparticles can passively target tumors via theenhanced permeability and retention (EPR) effect. Here, a combinedapproach is described in which the surface of a nanoparticle isdecorated with a urea-based small-molecule peptidomimetic inhibitor ofprostate specific membrane antigen (PSMA). This strategy takes advantageof both the avidity of the functionalized nanoparticle for binding toPSMA and the ability of the nanoparticle to be retained for longerperiods of time in the tumor due to enhanced leakage via EPR into thetumor interstitium and poor clearance due to underdeveloped ornon-existent lymphatics within the tumor. Previous baseline studies withnon-functionalized poly(lactide-β-ethylene glycol-β-lactide) (PEG-PLA)nanoparticles loaded with docetaxel demonstrated tumor regression inhuman PC3 prostate tumor xenografts. As an initial step to introducingthe targeting moiety, the amino terminus of the small-molecule PSMAinhibitor was conjugated to PEG (M_(n) 3400) bearing an activatedcarboxyl group to obtain a PEGylated inhibitor. Studies undertaken usinga radiolabeled PSMA-substrate based assay established that the PEGylatedinhibitor had an IC₅₀ value similar to the uncomplexed inhibitor.Subsequently, nanoparticles loaded with docetaxel were formulated usinga mixture of poly(lactide-β-ethylene glycol-β-lactide) andPSMA-inhibitor bound α-amino-ω-hydroxy terminated poly(ethyleneglycol-β-ε-caprolactone). In vitro studies using these nanoparticlesdemonstrated selective cytotoxicity against PSMA-producing cells.Binding of fluorescently labeled PSMA-targeted particles toPSMA-producing cells has also been directly observed using fluorescencemicroscopy and observed in secondary fashion using a PSMA substratebased enzyme inhibition assay.

Methods of the Invention

In one aspect, the invention provides a method for treating orpreventing a disease or disorder in a subject, the method comprising thestep of administering to the subject a nanoparticle composition, suchthat the administration of the nanoparticle composition is effective totreat or prevent said disease or disorder, wherein the nanoparticlecomposition comprises a) a prostate specific membrane antigen (PSMA)inhibitor; b) a linker, c) a biologically active agent; and d) ananoparticle; or a nanoparticle composition of formula I:

(X)_(m)—(Y)_(n)—Z  (I);

wherein

X is an organic small molecule PSMA inhibitor;

Y is an organic linker;

Z is a nanoparticle comprising a biologically active agent;

m is 1-1000 and

n is 1-1000.

In one embodiment, the disease is cancer or a proliferation disease.

In a further embodiment, the disease is cancer, tumor or carcinoma.

In certain embodiments, the disease is prostate cancer, bladder cancer,bone cancer, brain cancer, breast cancer, cervical cancer, colon cancer,epithelial cancers, esophageal cancer, gastrointestinal cancers, gallbladder cancer, gynecological cancers, kidney cancer, laryngeal cancer,liver cancer, lung cancer, nose cancer, ovarian cancer, pancreaticcancer, rectum cancer, Schneeberg lung cancer, skin cancer, squamus celland/or basal cell cancers, stomach cancer, testicular cancer, throatcancer, tongue cancer, urethral cancer, uterine cancer, vaginal cancer,cancer of the large intestine, cancer of the small intestine, cancer inthe area of the mouth and on the lip, brain tumors (gliomas), connectivetissue tumor, Ewing tumors, eye tumors, germ cell tumor, hypophysistumor, osteolytic tumors and osteoblastic tumors, soft tissue tumors,urological tumors, Wilm's tumor, tumors of the small intestine, tumorsof ear, nose and throat, head and neck tumors (tumors situated in theregion of the neck, nose and ears), tumor of the eyelid, acute myeloidleukemia (AML), acute promyelocytic leukemia (APL), adenocarcinomas,acute leukemia, acoustic neurinoma, ampullary carcinoma, anal carcinoma,astrocytomas, basal cell carcinoma, brain metastases, breast carcinoma,bronchial carcinoma, Burkitt's lymphoma, Canine B-Cell Lymphoma,carcinoids, choroidal melanoma, chronic myelogenous leukemia (CML),colorectal carcinoma, colon carcinoma, craniopharyngiomas, corpuscarcinoma, CUP syndrome, endometrial carcinoma, ependymoma, epithelialcall-derived neoplasia (epithelial carcinoma), esophageal carcinoma,gall carcinomas, glioblastomas, hairy cell leukemia, head and necksquamous cell carcinoma, hematological neoplasias, hepatocellularcarcinoma, Hodgkin's disease, Kaposi's sarcoma, liver metastases,leukemia, lymphomas, malignant lymphoma (Hodgkin/Non-Hodgkin), malignantmelanoma, malignant neoplasma, malignomas of the gastrointestinal tract,medulloblastomas, melanoma, meningiomas, mycosis fungoides, myelomas,neurinoma, neuroblastoma, Non-Hodgkin's lymphomas, non-small cellbronchial carcinoma, oligodendroglioma, osteosarcoma, ovarian carcinoma,pancreatic carcinoma, papillary renal carcinoma, penile carcinoma,plasmacytoma, prostate carcinoma, rectal carcinoma, renal cellcarcinoma, retinoblastoma, squamous cell carcinoma of the head and theneck, soft tissue sarcoma, spinocellular carcinoma, T-cell lymphoma(Mycosis fungoides), thymoma, thyroid carcinoma, tube carcinoma,urothelial carcinoma, vulvar carcinoma, wart appearance, and solidtumors.

In another embodiment, the disease is cancer, wherein the cancercomprises a neovasculature expressing PSMA.

In certain embodiments, the disease is prostate cancer, renal cellcarcinoma, glioblastoma, colon cancer, gastric cancer, bladder cancer,pancreatic cancer, sarcoma, melanoma, skin cancer and lung cancer.

In other embodiments, the disease is inflammation, arthritis, rheumatoidarthritis, spondylarthropathies, gouty arthritis, osteoarthritis,juvenile arthritis, and other arthritic conditions, systemic lupuserthematosus (SLE), skin-related conditions, psoriasis, eczema, burns,dermatitis, neuroinflammation, allergy, pain, neuropathic pain, fever,pulmonary disorders, lung inflammation, adult respiratory distresssyndrome, pulmonary sarcoisosis, asthma, silicosis, chronic pulmonaryinflammatory disease, and chronic obstructive pulmonary disease (COPD),cardiovascular disease, arteriosclerosis, myocardial infarction(including post-myocardial infarction indications), thrombosis,congestive heart failure, cardiac reperfusion injury, complicationsassociated with hypertension and/or heart failure, vascular organdamage, restenosis, cardiomyopathy, stroke, ischemic stroke, hemorrhagicstroke, reperfusion injury, renal reperfusion injury, ischemia, brainischemia, ischemia resulting from cardiac/coronary bypass,neurodegenerative disorders, liver disease and nephritis,gastrointestinal conditions, inflammatory bowel disease, Crohn'sdisease, gastritis, irritable bowel syndrome, ulcerative colitis,ulcerative diseases, gastric ulcers, viral and bacterial infections,sepsis, septic shock, gram negative sepsis, malaria, meningitis, HIVinfection, opportunistic infections, pneumonia, herpes virus, myalgiasdue to infection, influenza, autoimmune disease, graft vs. host reactionand allograft rejections, treatment of bone resorption diseases,osteoporosis, multiple sclerosis, angiogenesis including neoplasia,metastasis, central nervous system disorders, central nervous systemdisorders having an inflammatory or apoptotic component, Alzheimer'sdisease, Parkinson's disease, Huntington's disease, amyotrophic lateralsclerosis, spinal cord injury, and peripheral neuropathy.

In certain embodiments, the subject is administered an additionaltherapeutic agent.

In another embodiment, the compound and the additional therapeutic agentare administered simultaneously or sequentially.

In certain embodiments, the subject is a human, rat, mouse, cat, dog,horse, sheep, cow, monkey, avian, or amphibian. In a further embodiment,the subject is a human.

In one embodiment, the nanoparticle composition has an IC₅₀ valueranging from about 0.1 to about 200 nM.

In a further embodiment, the nanoparticle composition has an IC₅₀ valueranging from about 0.5 to about 125 nM.

In one aspect, the invention provides a method of synthesizing acompound of formula II in claim 5, comprising the steps of:

a) reacting a compound of formula A:

wherein,

R₁ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic;

R₂ is optionally substituted alkyl, optionally substituted alkenyl, oroptionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic;

R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄;

R₃ and R₄ are each independently selected at each occurrence from thefollowing: H, optionally substituted alkyl, optionally substitutedalkenyl or optionally substituted alkynyl, each containing 0, 1, 2, or 3heteroatoms selected from O, S, or N; optionally substituted aryl;optionally substituted heteroaryl; optionally substituted heterocyclic;or optionally substituted carbocyclic;

with a compound of formula B:

wherein

A is O, S, NH, N(alkyl) or N(aryl);

R_(A) is optionally substituted alkyl, optionally substituted alkenyl oroptionally substituted alkynyl, each containing heteroatoms selectedfrom O, S, or N; and

each LG is independently a leaving group; and

b) reacting the product of step a) with a nanoparticle comprising abiologically active agent to form a composition of formula II.

Typical subjects to which compounds of the invention may be administeredare mammals, particularly primates, especially humans. For veterinaryapplications, a wide variety of subjects are suitable, e.g. livestocksuch as cattle, sheep, goats, cows, swine and the like; poultry such aschickens, ducks, geese, turkeys, and the like; and domesticated animalsparticularly pets such as dogs and cats. For diagnostic or researchapplications, a wide variety of mammals are suitable subjects includingrodents (e.g. mice, rats, hamsters), rabbits, primates, and swine suchas inbred pigs and the like. Additionally, for in vitro applications,such as in vitro diagnostic and research applications, body fluids andcell samples of the above subjects are suitable for use such asmammalian, particularly primate such as human, blood, urine or tissuesamples, or blood urine or tissue samples of the animals mentioned forveterinary applications.

Pharmaceutical Compositions and Kits

In certain aspect, the invention provides a kit comprising ananoparticle composition, and instructions for use in treating cancer,wherein the nanoparticle composition comprises a) a prostate specificmembrane antigen (PSMA) inhibitor; b) a linker, c) a biologically activeagent; and d) a nanoparticle; or a nanoparticle composition of formulaI:

(X)_(m)—(Y)_(n)—Z  (I);

wherein

X is an organic small molecule PSMA inhibitor;

Y is an organic linker;

Z is a nanoparticle comprising a biologically active agent;

m is 1-1000 and

n is 1-1000.

In another aspect, the invention provides a pharmaceutical compositioncomprising a nanoparticle composition, and a pharmaceutically suitableexcipient, wherein the nanoparticle composition comprises a) a prostatespecific membrane antigen (PSMA) inhibitor; b) a linker, c) abiologically active agent; and d) a nanoparticle; or a nanoparticlecomposition of formula I:

(X)_(m)—(Y)_(n)—Z  (I);

wherein

X is an organic small molecule PSMA inhibitor;

Y is an organic linker;

Z is a nanoparticle comprising a biologically active agent;

m is 1-1000 and

n is 1-1000.

The present invention also provide packaged pharmaceutical compositionscomprising a pharmaceutical acceptable carrier and a composition of theinvention. In certain embodiments the packaged pharmaceuticalcomposition will comprise the reaction precursors necessary generate thecomposition of the invention upon combination of the biologically activeagent.

In certain preferred embodiments, the invention provides a kit accordingto the invention contains a composition of the invention, in combinationwith a pharmaceutically acceptable carrier. The composition and carriermay be provided in solution or in lyophilized form. When the compositionand carrier of the kit are in lyophilized form, the kit may optionallycontain a sterile and physiologically acceptable reconstitution mediumsuch as water, saline, buffered saline, and the like.

The kit may provide a composition of the invention in solution or inlyophilized form, and these components of the kit of the invention mayoptionally contain stabilizers such as NaCl, silicate, phosphatebuffers, ascorbic acid, gentisic acid, and the like. Additionalstabilization of kit components may be provided in this embodiment, forexample, by providing the reducing agent in an oxidation-resistant form.

Determination and optimization of such stabilizers and stabilizationmethods are well within the level of skill in the art. When thecomposition is in lyophilized form, the kit may optionally contain asterile and physiologically acceptable reconstitution medium such aswater, saline, buffered saline, and the like. The amounts ofcomposition, auxiliary molecule, and/or other reagents in thisembodiment are optimized in accordance with the methods set forth above.

The pharmaceutical compositions of the present invention comprise atherapeutically effective amount of a composition of the presentinvention formulated together with one or more pharmaceuticallyacceptable carriers. As used herein, the term “pharmaceuticallyacceptable carrier” means a non-toxic, inert solid, semi-solid or liquidfiller, diluent, encapsulating material or formulation auxiliary of anytype. The pharmaceutical compositions of this invention can beadministered to humans and other animals orally, rectally, parenterally,intracisternally, intravaginally, intraperitoneally, topically (as bypowders, ointments, or drops), buccally, or as an oral or nasal spray.

Liquid dosage forms for oral administration include pharmaceuticallyacceptable emulsions, microemulsions, solutions, suspensions, syrups andelixirs. In addition to the active compounds, the liquid dosage formsmay contain inert diluents commonly used in the art such as, forexample, water or other solvents, solubilizing agents and emulsifierssuch as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethylacetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyleneglycol, dimethylformamide, oils (in particular, cottonseed, groundnut,corn, germ, olive, castor, and sesame oils), glycerol,tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid estersof sorbitan, and mixtures thereof. Besides inert diluents, the oralcompositions can also include adjuvants such as wetting agents,emulsifying and suspending agents, sweetening, flavoring, and perfumingagents.

Injectable preparations, for example, sterile injectable aqueous oroleaginous suspensions may be formulated according to the known artusing suitable dispersing or wetting agents and suspending agents. Thesterile injectable preparation may also be a sterile injectablesolution, suspension or emulsion in a nontoxic parenterally acceptablediluent or solvent, for example, as a solution in 1,3-butanediol. Amongthe acceptable vehicles and solvents that may be employed are water,Ringer's solution, U.S.P. and isotonic sodium chloride solution. Inaddition, sterile, fixed oils are conventionally employed as a solventor suspending medium. For this purpose any bland fixed oil can beemployed including synthetic mono- or diglycerides. In addition, fattyacids such as oleic acid are used in the preparation of injectables.

In order to prolong the effect of a drug, it is often desirable to slowthe absorption of the drug from subcutaneous or intramuscular injection.This may be accomplished by the use of a liquid suspension ofcrystalline or amorphous material with poor water solubility. The rateof absorption of the drug then depends upon its rate of dissolutionwhich, in turn, may depend upon crystal size and crystalline form.Alternatively, delayed absorption of a parenterally administered drugform is accomplished by dissolving or suspending the drug in an oilvehicle.

Compositions for rectal or vaginal administration are preferablysuppositories which can be prepared by mixing the compounds of thisinvention with suitable non-irritating excipients or carriers such ascocoa butter, polyethylene glycol or a suppository wax which are solidat ambient temperature but liquid at body temperature and therefore meltin the rectum or vaginal cavity and release the active compound.

Solid compositions of a similar type may also be employed as fillers insoft and hard-filled gelatin capsules using such excipients as lactoseor milk sugar as well as high molecular weight polyethylene glycols andthe like.

The active composition can also be in micro-encapsulated form with oneor more excipients as noted above. The solid dosage forms of tablets,dragees, capsules, pills, and granules can be prepared with coatings andshells such as enteric coatings, release controlling coatings and othercoatings well known in the pharmaceutical formulating art. In such soliddosage forms the active compound may be admixed with at least one inertdiluent such as sucrose, lactose or starch. Such dosage forms may alsocomprise, as is normal practice, additional substances other than inertdiluents, e.g., tableting lubricants and other tableting aids such amagnesium stearate and microcrystalline cellulose. In the case ofcapsules, tablets and pills, the dosage forms may also comprisebuffering agents.

Dosage forms for topical or transdermal administration of a compound ofthis invention include ointments, pastes, creams, lotions, gels,powders, solutions, sprays, inhalants or patches. The active componentis admixed under sterile conditions with a pharmaceutically acceptablecarrier and any needed preservatives or buffers as may be required.Ophthalmic formulation, ear drops, eye ointments, powders and solutionsare also contemplated as being within the scope of this invention.

The ointments, pastes, creams and gels may contain, in addition to anactive compound of this invention, excipients such as animal andvegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulosederivatives, polyethylene glycols, silicones, bentonites, silicic acid,talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to the compounds of thisinvention, excipients such as lactose, talc, silicic acid, aluminumhydroxide, calcium silicates and polyamide powder, or mixtures of thesesubstances. Sprays can additionally contain customary propellants suchas chlorofluorohydrocarbons.

Transdermal patches have the added advantage of providing controlleddelivery of a compound to the body. Such dosage forms can be made bydissolving or dispensing the compound in the proper medium. Absorptionenhancers can also be used to increase the flux of the compound acrossthe skin. The rate can be controlled by either providing a ratecontrolling membrane or by dispersing the compound in a polymer matrixor gel.

As is well understood in the medical arts a therapeutically effectiveamount of a composition of this invention will be at a reasonablebenefit/risk ratio applicable to any medical treatment.

Binding of PEGylated Inhibitor, FPPi, to PSMA

The PSMA inhibitor PSMAi1 is ideally suited for this nanoparticleapplication due to the presence of a primary amine that allows for amidebond formation with carboxyl groups present on PEG monomers. Previouslyit had been demonstrated that urea-based PSMA inhibitors bearingstructural homology to PSMAi1 inhibited NAAG hydrolysis with the IC₅₀value range of 1-10 nM (Kozikowski, A. P., ET AL. J Med Chem, 47:1729-1738, 2004). On this basis, PSMAi1 was coupled to fluorescentlylabeled 3400 MW PEG as outlined in Scheme 1. The presence of thefluorescein at the opposite end of the PEG monomer allowed a way tofollow the reaction and subsequent purification of the product bydialysis. FPPi inhibited PSMA hydrolysis of NAAG with an IC₅₀ valuebetween 1 and 10 nM. While it was expected that the addition of thelarge PEG moiety to increase the IC₅₀ value, the IC₅₀ value was still inthe same range suggesting that a) the addition of PEG did not pose asteric hinderance and b) FPPi possessed sufficient affinity for PSMA tojustify further studies in which the PEGylated inhibitor would beintroduced onto the surface of nanoparticles. PEG itself was notobserved to bind to affect the enzymatic of PSMA (data not shown).

Nanoparticle Formulation

The synthesis of the PSMA-targeted nanoparticle was based on a strategywhereby the PLA-PEG-PLA copolymer partitions such that the PLA regionwould comprise the core of the nanoparticle while the water-soluble butacetone-insoluble PEG region would be in the aqueous layer and thusemerge on the surface. This approach has been defined earlier andprovides stealth attributes to the nanoparticle (Farokhzad, O. C., etal. Proc Natl Acad Sci USA, 103: 6315-6320, 2006; Hu, Y., et al.Biomaterials, 24: 2395-2404, 2003). Since the tricarboxylic acidcontaining PSMA inhibitor is highly hydrophilic, it would be expected toorient itself toward the surface of the nanoparticle during formulation.In order to facilitate such orientation, it was conjugated to thePEG-PCL copolymer such that the PCL would integrate into thenanoparticle matrix and the PEG and hydrophilic PSMAi2 would orienttoward the surface. On this basis, the polymer bound PSMA inhibitor(polyPSMAi2) was synthesized as outlined in Scheme 2. ¹H-NMR and ESIanalysis confirmed correct structure. Nanoparticles incorporatingpolyPSMAi2 (nanoPSMAi2) and docetaxel were then formulated using thesolvent evaporation technique. NanoPSMAi2 particles were found to bemonodisperse with a polydispersity index of 0.131 and had an averagesize of approximately 222 nm (FIG. 3). The loading efficiency ofdocetaxel was observed to be in the range of 40±2% over multipleexperiments. The surface density of the PSMA inhibitor was computed tobe 2.23×10¹⁷ molecules/m² of surface area of the nanoparticles (˜30,000inhibitor molecules/nanoparticle).

Nanoparticle Binding as Observed by NAAG Assay

Nanoparticles formulated with a surface decorated with small-moleculePSMA inhibitors were tested for activity against PSMA from LNCaPhomogenate via the NAAG assay as described above. Initial testing wascarried out with polyPSMAi2 which was observed to inhibit the activityof PSMA at an IC₅₀ of close to 1000 ng/mL. Subsequently, polyPSMAi2 wasincorporated into the nanoparticle matrix to give nanoPSMAi2, which wasalso observed to inhibit PSMA activity. A shift of the binding curve tothe right was observed, FIG. 2b , suggesting that when tethered on thesurface of the nanoparticle, the inhibitor is unable to bind to PSMAwith the same affinity as it could when in the polymeric form.

Observation of Nanoparticle Binding by Fluorescence

To evaluate whether the nanoPSMAi2 particles exhibited enhanced bindingto PSMA-positive prostate cancer cells compared to nontargeted nanoPEGparticles, the respective particles were labeled with Texas Red. Thiswas accomplished by incorporating a Texas Red labeled PEG-PCL copolymer(polyTR) into the nanoparticles. The incorporation of Texas Red (MW 625Da) labeled polymers was not expected to alter the size of thenanoparticles significantly. Since it is known that cells cannonspecifically endocytose polymer nanoparticles (Chavanpatil, M. D., etal. J Nanosci Nanotechnol, 6: 2651-2663, 2006), the concentration of thenanoparticles was kept low. The cells were also incubated with thenanoparticle suspension under agitation to further minimize endocytosis.

A confocal section of the nontargeted Texas Red labeled nanoPEGparticles exhibited no red fluorescence as would have been observed withnanoparticles binding to cells. In contrast, the targeted nanoPSMAi2particles undergo endocytosis after 15 min of incubation. Previously itwas demonstrated that PSMA becomes internalized following binding byantibodies and small-molecule PSMA inhibitors (Rajasekaran, S. A., etal. Mol Biol Cell, 14: 4835-4845, 2003). PSMA can also undergointernalization and be recycled in the absence of ligand binding.Herein, minimal to no endocytosis was observed in the case of thenontargeted particles. Thus, it appears that the endocytosis is mediatedby nanoPSMAi2 particle binding to PSMA leading to subsequentinternalization by endocytosis.

In addition to confocal microscopy, fluorescence microscopy wasundertaken with the intention of observing nanoparticle binding on thecell surface. The data obtained suggest that binding on the cell surfaceis highly dependent on the presence of a targeting moiety on the surfaceof the nanoparticle. As expected, minimal nonspecific surface binding isobserved in the case of the nontargeted nanoparticles. In contrast, ahigh number of PSMA-targeted nanoparticles are seen on the cell surfaceaway from the nuclei.

In Vitro Cytotoxicity to PSMA Expressing Human Prostate Cancer Cells

Previously, Farokhzad et al compared the in vitro cytotoxicity ofdocetaxel encapsulated PSMA-targeted RNA aptamer nanoparticle to anontargeted nanoparticle to LNCaP cells (Farokhzad, O. C., et al. ProcNatl Acad Sci USA, 103: 6315-6320, 2006.). This group demonstrated that72 hrs after a 30 min exposure the viability of LNCaP cells exposed tothe PSMA-targeted particles was 20% higher than the nontargetedparticles. The cytotoxicity of the nontargeted particles in that studywas ascribed to a combination of nonspecific uptake and to the expectednonspecific release of docetaxel from the particle into the media overthe exposure period. To evaluate whether incorporation of the urea-basedPSMA inhibitor enhanced the cytotoxicity of the nanoparticle to PSMAexpressing cells in vitro, we performed similar assays to those ofFarokhzad et al and compared the effects of the docetaxel loadednanoPSMAi2 particles to those of the untargeted nanoPEG particles anddocetaxel alone. Following determination of the amount of docetaxelloading in the particles, PSMA-expressing LNCaP human prostate cancercells were exposed to equimolar amounts (i.e. 100 nM) of loadednanoparticles or free docetaxel. To minimize the effects of nonspecificendocytosis, cells were only exposed to test compounds for 15 min atwhich time cells were washed and then placed in drug free media. Cellcounts were determined by converting absorbance from MTT assay to cellnumber based on a standard curve of absorbance from MTT assay of knownamounts of LNCaP cells. In this assay, 48 hrs following exposure, thegrowth of cells exposed to the nontargeted nanoPEG particles wasinhibited by 65% while cell growth was inhibited 89% by docetaxel and95% by the nanoPSMAi2 particles. At 96 hrs after exposure to thenontargeted particles cells continued to grow but overall cell growthwas inhibited 70% compared to control. In contrast, at this time pointexposure to the nanoPSMAi2 particles resulted in a ˜10% decrease in theabsolute cell number compared to starting cell number at day 0, FIG. 4.These results demonstrate the increased antitumor efficacy that can beachieved by incorporating a cell surface protein specific binding ligandonto the surface of a docetaxel encapsulated nanoparticle. No efficacywas observed in any of the abovementioned systems at a concentration ofdocetaxel of 10 nM.

In these studies it has been established that a nanoparticle systemdecorated with a small-molecule PSMA inhibitor on the surface enhancesbinding to PSMA. This is the first time in our knowledge that such asystem has been designed with the use of small-molecule ligands for PSMAas a specificity-conferring mechanism. The approach is comparable to theapproach of Farokhzad et al. who characterized a docetaxel encapsulatedPSMA-targeted RNA aptamer based nanoparticle for in vitro toxicity andfor efficacy following intratumoral injection in vivo. Those authorsselected a previously described RNA aptamer A10, which is a competitiveinhibitor with a reported K_(i) for PSMA of 11.9 nM (Lupold, S. E., etal. Cancer Res, 62: 4029-4033, 2002). The urea-based inhibitor used totarget our particles has a K_(i) value in a similar range. Other groupshave conjugated anti-PSMA antibodies to nanoparticles in order togenerate systems that could be used for both imaging and therapeuticapplications (Gao, X., et al. Nat Biotechnol, 22: 969-976, 2004).

Using a small-molecule inhibitor based system has certain uniqueadvantages. First, the chemistry can be more controlled because unlikeantibodies or aptamers, small-molecules can be synthesized with higherpurity, accuracy, efficiency and economy. Another reason as compared toantibodies and aptamers is that unlike antibodies, small-molecules donot need to form tertiary structures to facilitate binding. Thusstability during formulation, which can be a big factor, is not an issuein this case. The use of a small-molecule inhibitor is advantageoussince it has a lower exclusion space suggesting that up to 30,000inhibitor molecules can be loaded on the surface (as observed in thisstudy) thus maximizing the possibility of binding. And finally, in termsof future in vivo experiments, small-molecules are less likely to elicitan immune response compared to large antibodies, and therefore suchnanoparticles should provide long circulatory half lives in the bodyupon injection.

The results demonstrate that PSMA-targeted nanoparticles enhancecytotoxicity via binding to PSMA protein present on the surface ofprostate cancer cells.

EXAMPLES

The present invention is further illustrated by the following exampleswhich should not be construed as limiting in any way. The practice ofthe present invention will employ, unless otherwise indicated,conventional techniques, which are within the skill of the art. Suchtechniques are explained fully in the literature.

General Procedures.

All reactions were performed under a nitrogen atmosphere unlessotherwise noted. Solvents and chemicals obtained from commercial sourceswere of analytical grade or better and used without furtherpurification. All experiments were performed in duplicate or triplicateto ensure reproducibility. Analytical thin-layer chromatography (TLC)was performed using Aldrich aluminum-backed 0.2 mm silica gel Z19, 329-1plates and visualized by ultraviolet light (254 nm), I₂ and 1% ninhydrinin EtOH. Flash chromatography was performed using silica gel purchasedfrom Bodman (Aston Pa.), MP SiliTech 32-63 D 60 Å. In most cases productisolation consisted of removing of the solvent from the reactionmixture, extracting with an organic solvent, washing with water andbrine, drying with anhydrous sodium sulfate, filtering, andconcentrating the filtrate. The use of such workup conditions will beindicated by the phrase “product isolation” (which is followed, inparentheses, by the extracting solvent). Purification in most cases wasachieved by flash chromatography and is signified by the term “flashchromatography” (which is followed, in parentheses, by the elutionsolvent used). Melting points were measured using a Mel-Temp apparatusand are uncorrected. ¹H NMR spectra were recorded on either a VarianMercury 400 MHz or on a Bruker Ultrashield™ 400 MHz spectrometer.Chemical shifts (6) are reported in ppm downfield by reference to protonresonances resulting from incomplete deuteration of the NMR solvent. Lowresolution ESI mass spectra were obtained on a Bruker Daltonics Esquire3000 Plus spectrometer. Higher-resolution FAB mass spectra were obtainedon a JOEL JMS-AX505HA mass spectrometer in the mass spectrometerfacility at the University of Notre Dame. Optical rotation was measuredon a Jasco P-1010 polarimeter. Infrared spectra were obtained on aBruker Tensor 27 spectrometer.

Materials and Methods

Fluor-PEG-NHS (Nektar Therapeutics, Ala.) was used as purchased. Allother polymers were purchased from Polymer Source (Canada). They wereused as instructed by the manufacturer. Tetronic 904 surfactant was akind gift from BASF (Florham Park, N.J.). Unless otherwise described,all chemicals were purchased from Sigma Aldrich (Saint Louis, Mo.), andused without any further purification.

Cell Lines

LNCaP human prostate cancer cell lines used in this study were purchasedfrom ATCC and grown in RPMI 1640 supplemented with 10% fetal bovineserum (HyClone, Utah), 1% penicillin-streptomycin (Mediatech, Va.), and1% L-glutamine (Mediatech, Va.). The cells were maintained at 37° C. ina humidified 5% CO₂-containing incubator.

Example 1

Synthesis of PEGylated PSMA inhibitor (FPPi)

To a solution of 2-[3-(5-amino-1-carboxypentyl)-ureido]-pentanedioicacid (PSMAi1) (38 mg, 88.2 μmol in 1.5 mL dimethylformamide) was addeddiisopropylethylamine (0.3 mL, 1.72 mmol) followed by Fluor-PEG-NHS (MW˜3400) solution (150 mg, 44.11 μmol in 1 mL dimethylformamide) at 0° C.(Scheme 1). After 5 min, the solution was allowed to warm to roomtemperature and was kept for 16 h under an argon atmosphere. Thesolution was concentrated under high vacuum to yield a yellow residue.The residue was dissolved in 10 mL of methylene chloride and washed with5×10 mL of water to remove the starting material. Organic fractions werecombined and concentrated under reduced pressure to yield a yellowsolid. The solid FPPi was further purified by dialysis against waterusing a MW 1000 cutoff membrane (SpectraPOR CE, CA) using 3 solventchanges over 4 days, followed by lyophilization for further use. FPPiwas characterized by ¹H-NMR.

Example 2

Synthesis of NHS ester of PSMA inhibitor,2-(3-{1-carboxy-5-[7-(2,5-dioxo-pyrrolidin-1-yloxycarbonyl)-heptanoylamino]-pentyl}-ureido)-pentanedioicacid (PSMAi2)

2-{3-[5-[7-(2,5-dioxo-pyrrolidin-1-yloxycarbonyl)-heptanoylamino]-1-(4-methoxy-benzyloxycarbonyl)-pentyl]-ureido}-pentanedioicacid bis-(4-methoxy-benzyl) ester (30 mg, 0.032 mmol) was dissolved in 5mL 1:1 TFA:methylene chloride solution and was kept at room temperaturefor 3 h (Scheme 2). The resulting solution was evaporated under reducedpressure. The colorless solid residue was washed 5×1 mL of diethylether. The residue was dissolved in 10 mL chloroform and extracted with3×10 mL water to remove impurities. The organic layer was evaporated todryness to get the desired product, PSMAi2. Yield: 11.4 mg, 62%. Productwas characterized by ¹H NMR and MALDI-TOF.

Example 3

Coupling of PSMAi2 to PEG-PCL (polyPSMAi2)

PSMAi2 (11.4 mg, 20 μmol) was dissolved in 3 mL dimethylformamide (DMF).PEG-PCL (MW-25000, ratio of PEG:PCL is approximately 1:4 by weight) (257mg, 10 μmol in 5 mL DMF) was added at room temperature followed bydiisopropylethylamine (0.5 mL) and was kept at room temperature for 48hr (Scheme 3). The resulting solution was concentrated under vacuum anda white solid was then precipitated by dropwise addition to water. Theprecipitate was redissolved in DMF, precipitated again in water and thenwashed with 5×10 mL methanol. All organic fractions were combinedtogether and evaporated under reduced pressure. The desired product wasobtained as a colorless solid and characterized by ¹H-NMR.

Example 4

Synthesis of Texas Red Labeled PEG-PCL (polyTR)

115 mg (4.6 μmol) of PEG-PCL was dried overnight under high vacuum.Texas Red sulfonyl chloride (3 mg, 4.8 μmol in 1 mL of dry DMF and 0.1mL diisopropylethylamine) was then added to PEG-PCL under N₂ withvigorous stirring. The reaction was allowed to proceed overnight in thedark at room temperature. Separation of the labeled copolymer wasachieved by precipitation in water. Further purification was achieved byredissolving in DMF followed by reprecipitation and washing with 5×10 mLof water. Final product, polyTR was obtained as a lyophilized solid andcharacterized by fluorescence.

Example 5 Formulation and Characterization of Nanoparticles

Polymer nanoparticles were formulated as a modification of the solventevaporation technique as described previously (Hu, Y., et al.Biomaterials, 24: 2395-2404, 2003). Briefly, nanoparticles were preparedby initially dissolving 5 μL of 100 mg/mL docetaxel in DMSO into 5 mL ofa 10 mg/mL solution of PLA-PEG-PLA. PLA-PEG-PLA comprised of a 1.2 kDachain of PEG flanked by a 6.3 kDa chain of PLA on either side. Thepolymer was nanoprecipitated along with the encapsulated drug by slowlypipetting into 10 mL of a 0.4% solution of Tetronic 904 with vigorousagitation for approximately 15 min. Subsequently, the acetone wasevaporated under a rotary evaporator taking care to prevent excessivebumping in the round bottomed flask. The polymer nanoparticles wereseparated by centrifuging at 10000 g for 15 min. This was repeated once.The nanoparticles were finally redispersed in Tetronic 904 depending onthe desired final concentration of docetaxel. Targeted nanoparticleswere formulated in a similar fashion with the exception that thepolyPSMAi was incorporated into the nanoparticle by initially dissolvingit with PLA-PEG-PLA in acetone such that a known ratio of polyPSMAi toPLA-PEG-PLA was maintained. When fluorescent particles were desired,polyTR was added in a manner akin to the polyPSMAi.

Particle size was determined using a Zetasizer (Malvern Zetasizer 3000,Malvern, UK). Each analysis lasted until a suitable value for theauto-correlation function was obtained and was performed at 25° C. Themeasurement was repeated three times with the average size across themeasurements being reported.

Surface coverage of PSMA inhibitor on the nanoparticles was determinedby ¹H-NMR. Targeted nanoparticles were dissolved in CHCl₃ and NMRspectra were obtained. The ratio of the proton peak at 5.2 ppm from thepolycaprolactone to the peak at 4.1 from the polylactic acid provided uswith a measure of integration of the polyPSMAi into the PLA-PEG-PLAcopolymer mesh. Given that the yield of the reaction in which the PSMAinhibitor was conjugated to PEG-PCL was previously evaluated, it waspossible to determine the number of PSMA inhibitor molecules per gram ofpolymer. With the assumption that the particles have a specific gravityof 1, and with knowledge of the particle size, the surface coverage canbe computed.

Example 6 Determination of Drug Loading

High performance liquid chromatography (HPLC) analysis was carried outusing a C-18 column on a reversed phase HPLC system (Waters, Mass.). Adual-absorbance detector (Waters 2457) was used for analysis at 215 nmand 254 nm. The mobile phase consisted of solvent A, 0.1% TFA in waterand solvent B, 0.1% TFA in acetonitrile. Gradient elution from 20% B to100% B over 22 minutes was used for chromatography. Chrom Perfectsoftware supplied with the HPLC system was used for data analysis. Acalibration curve for docetaxel was initially generated by injectingknown amounts of docetaxel and measuring the area under the elutioncurve at 254 nm. The area under the curve was fitted to the injectionamount in a linear fashion. To determine the amount of encapsulated drugin the nanoparticles, a known amount of drug-loaded nanoparticles wasdissolved in DMSO followed by injection onto the HPLC. The area underthe curve of the elution profile corresponding to docetaxel was measuredand the amount of docetaxel was estimated using the standard curve.Using the initial amount loaded onto the nanoparticles, the loadingefficiency was computed.

Example 7

N-acetylated-aspartyl-^([3H])glutamic acid (NAAG) assay for PSMAactivity

The NAAG assay involves measuring the cleavage of 50 nM NAAG by PSMA asdefined in earlier work (Denmeade, S. R., et al. Prostate, 54: 249-257,2003), in which the tritiated glutamic acid is released afterhydrolysis. The reaction was carried out in a microfuge tube. At thedesired time point, a known volume of the NAAG containing released^([3H])glutamic acid was added to an ion-exchange column. The released^([3H])glutamic acid binds to the column and is eluted by using 0.1Mformic acid. Degree of release of ^([3H])glutamic acid was measured byscintillation counting and is a direct measure of the release of productafter enzymatic reaction. LNCaP cell homogenate containing 2.8 ug/mL ofprotein was used as the source of PSMA for inhibition studies.PSMA-containing LNCaP homogenates were incubated with either inhibitor,nontargeted nanoparticles or targeted nanoparticles. The IC₅₀ value, asobtained from this study, is a measure of 50% inhibition of the activityof PSMA as compared to the activity in the absence of inhibitor.

Example 8 Confocal Microscopy

LNCaP cells were incubated with Cell Tracker Green (Molecular Probes,OR) at a concentration of 5 mM in buffer for 15 min, after which theywere washed with media to remove unreacted dye. The cells were thenstripped off the flask by using a final concentration of 2.5 mM of EDTAfor 15 min. Cells were collected, spun down, resuspended in media andstored in the incubator for 15 min followed by incubation with targetedor untargeted nanoparticles. Both nanoparticles were labeled with TexasRed. The degree of fluorescence from both nanoparticle systems wasestimated by measurement of fluorescence of a known concentration ofnanoparticles under a fluorescence plate reader (DTX880, BeckmanCoulter, Calif.). Cells were separated from the nanoparticles bycentrifuging at 300 g for 5 min. Spinning was repeated to remove allunbound nanoparticles from the cell suspension, following which cellswere plated on glass bottom petridishes (MatTek Corporation, MA) andvisualized using a Utraview LCI (Perkin Elmer, Mass.) confocalmicroscope equipped with Spinning Nipkow disk with microlenses. Cellswere viewed using a 100× objective. Images were captured in the temporalmodule using a LSI-cooled 12-bit CCD camera at 488 nm and 654 nmrespectively. Images were processed using the NIH ImageJ software(http://rsb.info.nih.gov/ij/download.html).

Example 9 Fluorescence Microscopy

LNCaP cells were stained with 4′,6-diamidino-2-phenylindole (DAPI)(Invitrogen, CA) for 5 min following which the excess dye was removed.Further incubation with nanoparticles was undertaken as described abovefor confocal microscopy. Cells were mounted on slides followed byimaging using a Nikon Eclipse E800 system (Santa Clara, Calif.) under100× magnification. Three representative fields per slide with twoslides for each condition were used.

Example 10 In Vitro Toxicity of Nanoparticles

Cytotoxicity assays were performed as described previously (Denmeade, S.R., et al. J Natl Cancer Inst, 95: 990-1000, 2003). Approximately 20,000LNCaP cells were seeded in 96-well plates and permitted to attach fortwo days. These cells were then incubated with 100 μL of a suspension ofdocetaxel loaded nanoparticles to a final concentration of 100 nMdocetaxel. After a 15 min exposure, the media and nanoparticles in allof the wells were carefully removed by pipetting to minimize celldetachment, followed by gentle washing with 200 μL of media. Cells werethen incubated in media at 37° C. and at the end of 48 hours and 96hours, effects on cell growth were determined using the MTT assay(Promega, Wis.) according to manufacturer's instructions.

The invention and the manner and process of making and using it, are nowdescribed in such full, clear, concise and exact terms as to enable anyperson skilled in the art to which it pertains, to make and use thesame. It is to be understood that the foregoing describes preferredembodiments of the present invention and that modifications may be madetherein without departing from the spirit or scope of the presentinvention as set forth in the claims. To particularly point out anddistinctly claim the subject matter regarded as invention, the followingclaims conclude this specification.

The contents of all cited references (including literature references,issued patents, published patent applications) as cited throughout thisapplication are hereby expressly incorporated by reference.

1. A nanoparticle composition comprising, a) a prostate specificmembrane antigen (PSMA) inhibitor; b) a linker, c) a biologically activeagent; and d) a nanoparticle.
 2. The composition of claim 1, wherein thePSMA inhibitor is attached to a linker.
 3. The composition of claim 1,wherein the biologically active agent is encapsulated in thenanoparticle.
 4. The composition of claim 1, wherein the linker isattached to the nanoparticle.
 5. A nanoparticle composition of formulaI:(X)_(m)(Y)_(n)—Z  (I); wherein X is an organic small molecule PSMAinhibitor; Y is an organic linker; Z is a nanoparticle comprising abiologically active agent; m is 1-1000 and n is 1-1000.
 6. Thecomposition of claim 5, wherein X is a compound of formula II,

wherein, R₁ is optionally substituted alkyl, optionally substitutedalkenyl, or optionally substituted alkynyl, each containing 0, 1, 2, or3 heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic; R₂ is optionally substitutedalkyl, optionally substituted alkenyl, or optionally substitutedalkynyl, each containing 0, 1, 2, or 3 heteroatoms selected from O, S,or N; optionally substituted aryl, optionally substituted arylalkyl,optionally substituted alkoxy, optionally substituted heteroaryl,optionally substituted heterocyclic, optionally substitutedalkylcarboxy, or optionally substituted carbocyclic; R′ and R″ are eachindependently —OR₄, —SR₄, —SOR₄, —SO₂R₄, —N(R₃)S(O)₂—R₄,—N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄, —C(O)NR₃R₄, or—N(R₃)C(O)R₄; R₃ and R₄ are each independently selected at eachoccurrence from the following: H, optionally substituted alkyl,optionally substituted alkenyl or optionally substituted alkynyl, eachcontaining 0, 1, 2, or 3 heteroatoms selected from O, S, or N;optionally substituted aryl; optionally substituted heteroaryl;optionally substituted heterocyclic; or optionally substitutedcarbocyclic; or a pharmaceutically acceptable salt thereof. 7-18.(canceled)
 19. The composition of claim 5, wherein Y is

wherein A is O, S, NH, N(alkyl) or N(aryl); and R_(A) is optionallysubstituted alkyl, optionally substituted alkenyl or optionallysubstituted alkynyl, each containing heteroatoms selected from O, S, orN. 20-30. (canceled)
 31. The composition of claim 5, wherein thebiologically active agent is selected from an anti-AIDS agent,anti-cancer agent, antibiotic, antioxidants, immunosuppressant,anti-viral agent, enzyme inhibitor, protease inhibitor, reversetranscriptase inhibitor, fusion inhibitor, neurotoxin, opiod, hypnotic,anti-histamine, lubricant, tranquilizer, anti-convulsant, musclerelaxant, anti-Parkinson agent, anti-spasmodic, muscle contractant,channel blocker, miotic, anti-cholinergic, anti-glaucoma agent,anti-parasite, anti-protozoal, modulator of cell-extracellular matrixinteraction, cell growth inhibitor, anti-adhesion agent, vasodilatingagent, inhibitor of DNA, inhibitor of RNA, inhibitor of proteinsynthesis, inhibitors of apoptotic genes, modulators of transcriptionfactors, anti-hypertensive, analgesic, anti-pyretic, steroidalanti-inflammatory agent, non steroidal anti-inflammatory agent,anti-angiogenic, anti-secretory, anticoagulant, antithrombotic agent,local anesthetic, ophthalmic, prostaglandin, anti-depressant,anti-psychotic, anti-emetic, antiproliferative, antimigration,antiangiogenic, antithrombotic, anti-inflammatory, antiphlogistic,cytostatic, cytotoxic, anticoagulative, antibacterial, antiviral and/orantimycotic agent and an imaging agent. 32-33. (canceled)
 34. Thecomposition of claim 5, of formula III:

wherein, R₁ is optionally substituted alkyl, optionally substitutedalkenyl, or optionally substituted alkynyl, each containing 0, 1, 2, or3 heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic; R₂ is optionally substitutedalkyl, optionally substituted alkenyl, or optionally substitutedalkynyl, each containing 0, 1, 2, or 3 heteroatoms selected from O, S,or N; optionally substituted aryl, optionally substituted arylalkyl,optionally substituted alkoxy, optionally substituted heteroaryl,optionally substituted heterocyclic, optionally substitutedalkylcarboxy, or optionally substituted carbocyclic; R′ and R″ are eachindependently —OR₄, —SR₄, —SOR₄, —SO₂R₄, —N(R₃)S(O)₂—R₄,—N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄, —C(O)NR₃R₄, or—N(R₃)C(O)R₄; R₃ and R₄ are each independently selected at eachoccurrence from the following: H, optionally substituted alkyl,optionally substituted alkenyl or optionally substituted alkynyl, eachcontaining 0, 1, 2, or 3 heteroatoms selected from O, S, or N;optionally substituted aryl; optionally substituted heteroaryl;optionally substituted heterocyclic; or optionally substitutedcarbocyclic; A is O, S, NH, N(alkyl) or N(aryl); and R_(A) is optionallysubstituted alkyl, optionally substituted alkenyl or optionallysubstituted alkynyl, each containing heteroatoms selected from O, S, orN; Z is a nanoparticle comprising a biologically active agent; and q is1-1000; or a pharmaceutically acceptable salt thereof. 35-44. (canceled)45. The composition of claim 5, of formula IV:

wherein, R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄; R₃ and R₄ are each independently selectedat each occurrence from the following: H, optionally substituted alkyl,optionally substituted alkenyl or optionally substituted alkynyl, eachcontaining 0, 1, 2, or 3 heteroatoms selected from O, S, or N;optionally substituted aryl; optionally substituted heteroaryl;optionally substituted heterocyclic; or optionally substitutedcarbocyclic; R_(A) is optionally substituted alkyl, optionallysubstituted alkenyl or optionally substituted alkynyl, each containingheteroatoms selected from O, S, or N; Z is a nanoparticle comprising abiologically active agent; and q is 1-1000; or a pharmaceuticallyacceptable salt thereof. 46-49. (canceled)
 50. A method for treating orpreventing a disease or disorder in a subject, the method comprising thestep of administering to the subject a nanoparticle composition of claim1, such that the administration of the nanoparticle composition iseffective to treat or prevent said disease or disorder.
 51. The methodof claim 50, wherein the disease is cancer or a proliferation disease.52. The method of claim 51, wherein the disease is cancer, tumor orcarcinoma.
 53. The method of claim 52, wherein the disease is prostatecancer, bladder cancer, bone cancer, brain cancer, breast cancer,cervical cancer, colon cancer, epithelial cancers, esophageal cancer,gastrointestinal cancers, gall bladder cancer, gynecological cancers,kidney cancer, laryngeal cancer, liver cancer, lung cancer, nose cancer,ovarian cancer, pancreatic cancer, rectum cancer, Schneeberg lungcancer, skin cancer, squamus cell and/or basal cell cancers, stomachcancer, testicular cancer, throat cancer, tongue cancer, urethralcancer, uterine cancer, vaginal cancer, cancer of the large intestine,cancer of the small intestine, cancer in the area of the mouth and onthe lip, brain tumors (gliomas), connective tissue tumor, Ewing tumors,eye tumors, germ cell tumor, hypophysis tumor, osteolytic tumors andosteoblastic tumors, soft tissue tumors, urological tumors, Wilm'stumor, tumors of the small intestine, tumors of ear, nose and throat,head and neck tumors (tumors situated in the region of the neck, noseand ears), tumor of the eyelid, acute myeloid leukemia (AML), acutepromyelocytic leukemia (APL), adenocarcinomas, acute leukemia, acousticneurinoma, ampullary carcinoma, anal carcinoma, astrocytomas, basal cellcarcinoma, brain metastases, breast carcinoma, bronchial carcinoma,Burkitt's lymphoma, Canine B-Cell Lymphoma, carcinoids, choroidalmelanoma, chronic myelogenous leukemia (CML), colorectal carcinoma,colon carcinoma, craniopharyngiomas, corpus carcinoma, CUP syndrome,endometrial carcinoma, ependymoma, epithelial call-derived neoplasia(epithelial carcinoma), esophageal carcinoma, gall carcinomas,glioblastomas, hairy cell leukemia, head and neck squamous cellcarcinoma, hematological neoplasias, hepatocellular carcinoma, Hodgkin'sdisease, Kaposi's sarcoma, liver metastases, leukemia, lymphomas,malignant lymphoma (Hodgkin/Non-Hodgkin), malignant melanoma, malignantneoplasma, malignomas of the gastrointestinal tract, medulloblastomas,melanoma, meningiomas, mycosis fungoides, myelomas, neurinoma,neuroblastoma, Non-Hodgkin's lymphomas, non-small cell bronchialcarcinoma, oligodendroglioma, osteosarcoma, ovarian carcinoma,pancreatic carcinoma, papillary renal carcinoma, penile carcinoma,plasmacytoma, prostate carcinoma, rectal carcinoma, renal cellcarcinoma, retinoblastoma, squamous cell carcinoma of the head and theneck, soft tissue sarcoma, spinocellular carcinoma, T-cell lymphoma(Mycosis fungoides), thymoma, thyroid carcinoma, tube carcinoma,urothelial carcinoma, vulvar carcinoma, wart appearance, and solidtumors. 54-62. (canceled)
 63. A kit comprising a nanoparticlecomposition of claim 1, and instructions for use in treating cancer. 64.A pharmaceutical composition comprising a nanoparticle composition ofclaim 1, and a pharmaceutically suitable excipient.
 65. A method ofsynthesizing a compound of formula II in claim 5, comprising the stepsof: a) reacting a compound of formula A:

wherein, R₁ is optionally substituted alkyl, optionally substitutedalkenyl, or optionally substituted alkynyl, each containing 0, 1, 2, or3 heteroatoms selected from O, S, or N; optionally substituted aryl,optionally substituted arylalkyl, optionally substituted alkoxy,optionally substituted heteroaryl, optionally substituted heterocyclic,or optionally substituted carbocyclic; R₂ is optionally substitutedalkyl, optionally substituted alkenyl, or optionally substitutedalkynyl, each containing 0, 1, 2, or 3 heteroatoms selected from O, S,or N; optionally substituted aryl, optionally substituted arylalkyl,optionally substituted alkoxy, optionally substituted heteroaryl,optionally substituted heterocyclic, or optionally substitutedcarbocyclic; R′ and R″ are each independently —OR₄, —SR₄, —SOR₄, —SO₂R₄,—N(R₃)S(O)₂—R₄, —N(R₃)(SO₂)NR₃R₄, —NR₃R₄, —C(O)—O—R₄, —C(O)R₄,—C(O)NR₃R₄, or —N(R₃)C(O)R₄; R₃ and R₄ are each independently selectedat each occurrence from the following: H, optionally substituted alkyl,optionally substituted alkenyl or optionally substituted alkynyl, eachcontaining 0, 1, 2, or 3 heteroatoms selected from O, S, or N;optionally substituted aryl; optionally substituted heteroaryl;optionally substituted heterocyclic; or optionally substitutedcarbocyclic; with a compound of formula B:

wherein A is O, S, NH, N(alkyl) or N(aryl); R_(A) is optionallysubstituted alkyl, optionally substituted alkenyl or optionallysubstituted alkynyl, each containing heteroatoms selected from O, S, orN; and each LG is independently a leaving group; and b) reacting theproduct of step a) with a nanoparticle comprising a biologically activeagent to form a composition of formula II.
 66. A method for treating orpreventing a disease or disorder in a subject, the method comprising thestep of administering to the subject a nanoparticle composition of claim5, such that the administration of the nanoparticle composition iseffective to treat or prevent said disease or disorder.
 67. A kitcomprising a nanoparticle composition of claim 5, and instructions foruse in treating cancer.
 68. A pharmaceutical composition comprising ananoparticle composition of claim 5, and a pharmaceutically suitableexcipient.